How does one visualise $DNA$ on an agarose gel?

  • A
    By using $X$-ray diffraction
  • B
    By staining with Ethidium Bromide followed by exposure to $UV$ light
  • C
    By staining with Coomassie blue followed by exposure to $UV$ light
  • D
    By using infrared light

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Agarose gel electrophoresis is used to separate $DNA$ fragments. The $DNA$ fragments separate due to . . . . . . .

Bacterial colonies that have a foreign $\text{DNA}$ fragment inserted into the plasmid will appear white,because $-$

$A$ number of bacteria with recombinant $DNA$ of the same type form:

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What is the criterion for the movement of $DNA$ fragments on an agarose gel during gel electrophoresis?

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